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Tag: Pharmaceutical manufacturing

Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation

Posted on May 27, 2025 By Admin

Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation Introduction: In the realm of pharmaceutical manufacturing, bilayer tablets have emerged as a significant advancement, offering multiple benefits such as the ability to combine incompatible substances, controlled release profiles, and patient convenience. However, the manufacturing…

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Solid Dosage form, Tablets

Addressing Failures in Weight Variation Control During Compression Equipment Validation

Posted on May 26, 2025 By Admin

Addressing Failures in Weight Variation Control During Compression Equipment Validation Addressing Failures in Weight Variation Control During Compression Equipment Validation Introduction: In the pharmaceutical industry, ensuring the consistency and quality of products is paramount, especially when it comes to solid dosage forms such as tablets. One critical aspect of tablet manufacturing is weight variation control…

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Solid Dosage form, Tablets

Validating Water for Injection (WFI) Systems in Multi-Product Facilities

Posted on May 26, 2025 By Admin

Validating Water for Injection (WFI) Systems in Multi-Product Facilities Validating Water for Injection (WFI) Systems in Multi-Product Facilities Introduction: Water for Injection (WFI) is a critical component in pharmaceutical manufacturing, particularly in multi-product facilities where diverse formulations are produced. WFI is used for dissolving or diluting substances or preparations during production, ensuring sterility and non-pyrogenicity….

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Solid Dosage form, Tablets

Addressing Punch Wear Issues During Tablet Press Validation

Posted on May 25, 2025 By Admin

Addressing Punch Wear Issues During Tablet Press Validation Addressing Punch Wear Issues During Tablet Press Validation Introduction: In the pharmaceutical manufacturing sector, ensuring the integrity and quality of tablet products is paramount. One critical aspect of this process is the validation of tablet presses, where punch wear can significantly impact product quality and efficiency. Punches,…

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Solid Dosage form, Tablets

Validating Batch Records for Regulatory Compliance in Tablet Manufacturing

Posted on May 25, 2025 By Admin

Validating Batch Records for Regulatory Compliance in Tablet Manufacturing Validating Batch Records for Regulatory Compliance in Tablet Manufacturing Introduction: In the pharmaceutical industry, ensuring the integrity and accuracy of batch records is paramount, particularly in the manufacturing of tablets. Batch records serve as a critical component in the documentation of each step of the manufacturing…

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Solid Dosage form, Tablets

Addressing Brittleness in Sugar-Coated Tablets During Validation Studies

Posted on May 25, 2025 By Admin

Addressing Brittleness in Sugar-Coated Tablets During Validation Studies Addressing Brittleness in Sugar-Coated Tablets During Validation Studies Introduction: Sugar-coated tablets have long been a popular choice in pharmaceutical manufacturing due to their aesthetic appeal, ease of swallowing, and ability to mask the taste of active ingredients. However, the process of sugar coating can introduce brittleness, posing…

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Solid Dosage form, Tablets

Addressing Residual Solvent Build-Up in Sugar-Coating Pans During Validation

Posted on May 25, 2025 By Admin

Addressing Residual Solvent Build-Up in Sugar-Coating Pans During Validation Addressing Residual Solvent Build-Up in Sugar-Coating Pans During Validation Introduction: The sugar-coating process in pharmaceutical manufacturing plays a crucial role in enhancing the aesthetic appeal, taste masking, and stability of tablets. However, managing residual solvent build-up during this process, particularly in the coating pans, is a…

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Solid Dosage form, Tablets

Troubleshooting Powder Segregation Issues During Validation of Compression Lines

Posted on May 25, 2025 By Admin

Troubleshooting Powder Segregation Issues During Validation of Compression Lines Troubleshooting Powder Segregation Issues During Validation of Compression Lines Introduction: In the realm of pharmaceutical manufacturing, maintaining the uniformity and consistency of solid dosage forms, such as tablets, is crucial. One of the common challenges faced during the validation of compression lines is powder segregation. This…

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Solid Dosage form, Tablets

Addressing Powder Bridging Issues in Tablet Press Feed Systems During Validation

Posted on May 24, 2025 By Admin

Addressing Powder Bridging Issues in Tablet Press Feed Systems During Validation Addressing Powder Bridging Issues in Tablet Press Feed Systems During Validation Introduction: In the pharmaceutical industry, ensuring the consistent production of high-quality tablets is paramount. The tablet press feed system plays a crucial role in this process by delivering a uniform and precise amount…

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Solid Dosage form, Tablets

Troubleshooting Label Application on Irregularly Shaped Tablet Bottles

Posted on May 23, 2025 By Admin

Troubleshooting Label Application on Irregularly Shaped Tablet Bottles Troubleshooting Label Application on Irregularly Shaped Tablet Bottles Introduction: In the pharmaceutical industry, the packaging of products is as critical as the formulation itself, ensuring safety, efficacy, and compliance. Labels on tablet bottles serve as the primary source of information for consumers and healthcare professionals, detailing everything…

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Solid Dosage form, Tablets

Managing Cross-Contamination Risks in Coating Machines Used for Extended Release Tablets

Posted on May 23, 2025 By Admin

Managing Cross-Contamination Risks in Coating Machines Used for Extended Release Tablets Managing Cross-Contamination Risks in Coating Machines Used for Extended Release Tablets Introduction: In the pharmaceutical industry, ensuring product safety and efficacy is paramount, and one critical aspect of this is managing cross-contamination risks. This is especially crucial in the production of extended-release tablets, where…

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Solid Dosage form, Tablets

Ensuring Consistency in Packaging Material Thickness for Stability

Posted on May 23, 2025 By Admin

Ensuring Consistency in Packaging Material Thickness for Stability Ensuring Consistency in Packaging Material Thickness for Stability Introduction: In the pharmaceutical industry, maintaining the stability of solid dosage forms like tablets is crucial. Packaging plays a vital role in ensuring product stability by protecting the contents from environmental factors such as moisture, oxygen, and light. Consistency…

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Solid Dosage form, Tablets

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  • Aerosol Formulations
  • Capsules (Hard & Soft Gelatin)
  • Drug Discovery
  • External Preparations
  • GLP Guidelines
  • GMP Guidelines
  • Medical Devices
  • Parenteral Drug Manufacturing
  • Pharma Quality Control
  • Pharma Research
  • Schedule M
  • Solid Dosage form
  • Solid Oral Dosage Forms
  • Tablets
  • Tablets

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